Canonical Allele Identifier: CA1818149077
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999201T= , CM000670.2:g.126999201T= GRCh38
NC_000008.10:g.128011446T= , CM000670.1:g.128011446T= GRCh37
NC_000008.9:g.128080628T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746076.2:n.1301-7354T=